Actively Recruiting
Conversion of Evidence and Applied Research on Intermittent Catheterization After Radical Hysterectomy
Led by West China Second University Hospital · Updated on 2024-07-31
70
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In this study, the investigators summarize the existing best evidence of intermittent catheterization in patients after radical cervical cancer surgery from the perspective of clinical translation of evidence through systematic search, evaluation and evidence integration, construct a nursing protocol of intermittent catheterization for patients after radical cervical cancer surgery based on the best evidence combined with the clinical context, and explore the clinical application effect of the above nursing protocol. It will provide a reference basis for the development of the standardization and management of intermittent catheterization for postoperative patients with cervical cancer in China, as well as the development of guidelines for intermittent catheterization after radical cervical cancer surgery.
CONDITIONS
Official Title
Conversion of Evidence and Applied Research on Intermittent Catheterization After Radical Hysterectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age
You will not qualify if you...
- Having serious diseases of the heart, brain, lungs, or other major organs
- Having water, electrolyte, or acid-base balance disorders at the start of intermittent catheterization
- Having previous serious kidney disease or bladder and urethra surgery
- Having a urinary tract infection
- Not completing all study interventions or data collection
- Voluntarily withdrawing from the study or death during the study period
- Refusing to participate in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
West China Second University Hospital, Sichuan University
Chengdu, Sichuan, China
Actively Recruiting
Research Team
L
Lu Xing
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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